ClearanceBrief
510(k) K072033 ยท EWO Audiometer

OTODYNAMICS OTOPORT

ApplicantOtodynamics, Ltd., Crofton MD, US
DecisionSubstantially Equivalent, Nov 13, 2007
ReceivedJul 24, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K072033

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.